Disease progression model for cognitive deterioration from Alzheimer's Disease Neuroimaging Initiative database

被引:91
作者
Ito, Kaori [1 ]
Corrigan, Brian [1 ]
Zhao, Qinying [1 ]
French, Jonathan [1 ]
Miller, Raymond [1 ]
Soares, Holly [1 ]
Katz, Elyse [1 ]
Nicholas, Timothy [1 ]
Billing, Bill [1 ]
Anziano, Richard [1 ]
Fullerton, Terence [1 ]
机构
[1] Pfizer Global Res & Dev, New London, CT USA
关键词
Disease progression model; Natural history; ADAS-cog; MCI; Alzheimer's disease; Age; APOE epsilon 4 genotype; CLINICAL PREDICTORS; RISK-FACTORS; IMPAIRMENT; DEMENTIA; DECLINE; SEX; AGE;
D O I
10.1016/j.jalz.2010.03.018
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: A mathematical model was developed to describe the longitudinal response in Alzheimer's Disease Assessment Scale-cognitive (ADAS-cog) obtained from the Alzheimer's Disease Neuroimaging Methods: The model was fit to the longitudinal ADAS-cog scores from 817 patients. Risk factors (age, apolipoprotein epsilon 4 [APOE epsilon 4] genotype, gentler, family history of AD, years of education) and baseline severity were tested as covariates. Results: Rate of disease progression increased with baseline severity. Age, APOE epsilon 4 genotype, and gender were identified as potential covariates influencing disease progression. The rate of disease progression in patients with mild to moderate AD was estimated as approximately 5.5 points/yr. Conclusions: A disease progression model adequately described the natural decline of ADAS-cog observed in Alzheimer's Disease Neuroimaging Initiative. Baseline severity is an important covariate to predict a curvilinear rate of disease progression in normal elderly, mild cognitive impairment, and AD patients. Age, APOE epsilon 4 genotype, and gender also influence the rate of disease progression. (C) 2011 The Alzheimer's Association. All rights reserved.
引用
收藏
页码:151 / 160
页数:10
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